Smith KD - Search Results

1

Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening.

Bezman L, Moser AB, Raymond GV, Rinaldo P, Watkins PA, Smith KD, Kass NE, Moser HW. Bezman L, et al. Among authors: smith kd. Ann Neurol. 2001 Apr;49(4):512-7. Ann Neurol. 2001. PMID: 11310629

2

A mouse model for X-linked adrenoleukodystrophy.

Lu JF, Lawler AM, Watkins PA, Powers JM, Moser AB, Moser HW, Smith KD. Lu JF, et al. Among authors: smith kd. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9366-71. doi: 10.1073/pnas.94.17.9366. Proc Natl Acad Sci U S A. 1997. PMID: 9256488 Free PMC article.

3

Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.

Kemp S, Wei HM, Lu JF, Braiterman LT, McGuinness MC, Moser AB, Watkins PA, Smith KD. Kemp S, et al. Among authors: smith kd. Nat Med. 1998 Nov;4(11):1261-8. doi: 10.1038/3242. Nat Med. 1998. PMID: 9809549

4

Pharmacological induction of peroxisomes in peroxisome biogenesis disorders.

Wei H, Kemp S, McGuinness MC, Moser AB, Smith KD. Wei H, et al. Among authors: smith kd. Ann Neurol. 2000 Mar;47(3):286-96. Ann Neurol. 2000. PMID: 10716247

5

Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described.

Lachtermacher MB, Seuánez HN, Moser AB, Moser HW, Smith KD. Lachtermacher MB, et al. Among authors: smith kd. Hum Mutat. 2000;15(4):348-53. doi: 10.1002/(SICI)1098-1004(200004)15:4<348::AID-HUMU7>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10737980

6

Altered expression of ALDP in X-linked adrenoleukodystrophy.

Watkins PA, Gould SJ, Smith MA, Braiterman LT, Wei HM, Kok F, Moser AB, Moser HW, Smith KD. Watkins PA, et al. Among authors: smith kd, smith ma. Am J Hum Genet. 1995 Aug;57(2):292-301. Am J Hum Genet. 1995. PMID: 7668254 Free PMC article.

7

Adrenoleukodystrophy: phenotypic variability and implications for therapy.

Moser HW, Moser AB, Smith KD, Bergin A, Borel J, Shankroff J, Stine OC, Merette C, Ott J, Krivit W, et al. Moser HW, et al. Among authors: smith kd. J Inherit Metab Dis. 1992;15(4):645-64. doi: 10.1007/BF01799621. J Inherit Metab Dis. 1992. PMID: 1528023 Review.

8

Tumor necrosis factor-alpha and X-linked adrenoleukodystrophy.

McGuinness MC, Griffin DE, Raymond GV, Washington CA, Moser HW, Smith KD. McGuinness MC, et al. Among authors: smith kd. J Neuroimmunol. 1995 Sep;61(2):161-9. doi: 10.1016/0165-5728(95)00084-f. J Neuroimmunol. 1995. PMID: 7593551 Free article.

9

Mouse very long-chain acyl-CoA synthetase in X-linked adrenoleukodystrophy.

Heinzer AK, Kemp S, Lu JF, Watkins PA, Smith KD. Heinzer AK, et al. Among authors: smith kd. J Biol Chem. 2002 Aug 9;277(32):28765-73. doi: 10.1074/jbc.M203053200. Epub 2002 Jun 4. J Biol Chem. 2002. PMID: 12048192 Free article.

10

A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.

Heinzer AK, Watkins PA, Lu JF, Kemp S, Moser AB, Li YY, Mihalik S, Powers JM, Smith KD. Heinzer AK, et al. Among authors: smith kd. Hum Mol Genet. 2003 May 15;12(10):1145-54. doi: 10.1093/hmg/ddg126. Hum Mol Genet. 2003. PMID: 12719378

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